1. Home
  2. Labeler Index
  3. Nomax Inc.
  4. 51801-008
  5. NDC Package Code: 51801-008-15 Dry Eye Test

NDC Package 51801-008-15 Dry Eye Test

Fluorescein Sodium Strip Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51801-008-15
Package Description:
50 POUCH in 1 CARTON / 2 STRIP in 1 POUCH
Product Code:
51801-008
Proprietary Name:
Dry Eye Test
Non-Proprietary Name:
Fluorescein Sodium
Substance Name:
Fluorescein Sodium
Usage Information:
For testing tear film stability by determining the fluorescein break-up time (FBUT).
11-Digit NDC Billing Format:
51801000815
Product Type:
Human Prescription Drug
Labeler Name:
Nomax Inc.
Dosage Form:
Strip - A long narrow piece of material.
Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • FLUORESCEIN SODIUM .12 mg/1
    • Pharmacologic Class(es):
  • Diagnostic Dye - [EPC] (Established Pharmacologic Class)
  • Dyes - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    12-05-2013
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51801-008-15?

    The NDC Packaged Code 51801-008-15 is assigned to a package of 50 pouch in 1 carton / 2 strip in 1 pouch of Dry Eye Test, a human prescription drug labeled by Nomax Inc.. The product's dosage form is strip and is administered via ophthalmic form.

    Is NDC 51801-008 included in the NDC Directory?

    Yes, Dry Eye Test with product code 51801-008 is active and included in the NDC Directory. The product was first marketed by Nomax Inc. on December 05, 2013 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51801-008-15?

    The 11-digit format is 51801000815. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-251801-008-155-4-251801-0008-15